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2.
Nat Commun ; 10(1): 2297, 2019 05 24.
Article in English | MEDLINE | ID: mdl-31127085

ABSTRACT

Candida albicans is a fungal pathobiont, able to cause epithelial cell damage and immune activation. These functions have been attributed to its secreted toxin, candidalysin, though the molecular mechanisms are poorly understood. Here, we identify epidermal growth factor receptor (EGFR) as a critical component of candidalysin-triggered immune responses. We find that both C. albicans and candidalysin activate human epithelial EGFR receptors and candidalysin-deficient fungal mutants poorly induce EGFR phosphorylation during murine oropharyngeal candidiasis. Furthermore, inhibition of EGFR impairs candidalysin-triggered MAPK signalling and release of neutrophil activating chemokines in vitro, and diminishes neutrophil recruitment, causing significant mortality in an EGFR-inhibited zebrafish swimbladder model of infection. Investigation into the mechanism of EGFR activation revealed the requirement of matrix metalloproteinases (MMPs), EGFR ligands and calcium. We thus identify a PAMP-independent mechanism of immune stimulation and highlight candidalysin and EGFR signalling components as potential targets for prophylactic and therapeutic intervention of mucosal candidiasis.


Subject(s)
Candida albicans/immunology , Fungal Proteins/immunology , Host-Pathogen Interactions/immunology , Air Sacs/microbiology , Animals , Candida albicans/genetics , Candida albicans/metabolism , Candidiasis/immunology , Candidiasis/microbiology , Cell Line, Tumor , Disease Models, Animal , Epithelial Cells/immunology , Epithelial Cells/metabolism , Epithelial Cells/microbiology , ErbB Receptors/genetics , ErbB Receptors/immunology , ErbB Receptors/metabolism , Female , Fungal Proteins/genetics , Fungal Proteins/metabolism , Humans , MAP Kinase Signaling System/immunology , Matrix Metalloproteinases/immunology , Matrix Metalloproteinases/metabolism , Mice , Mice, Inbred BALB C , Mucous Membrane/immunology , Mucous Membrane/microbiology , Pharyngitis/immunology , Pharyngitis/microbiology , Phosphorylation , Zebrafish
3.
Article in English | MEDLINE | ID: mdl-28775962

ABSTRACT

Vibrio vulnificus biotype 2-serovar E is a zoonotic clonal complex that can cause death by sepsis in humans and fish. Unlike other biotypes, Bt2 produces a unique type of MARTXVv (Multifunctional-Autoprocessive-Repeats-in-Toxin; RtxA13), which is encoded by a gene duplicated in the pVvBt2 plasmid and chromosome II. In this work, we analyzed the activity of this toxin and its role in human sepsis by performing in vitro, ex vivo, and in vivo assays. First, we demonstrated that the ACD domain, present exclusively in this toxin variant, effectively has an actin-cross-linking activity. Second, we determined that the whole toxin caused death of human endotheliocytes and monocytes by lysis and apoptosis, respectively. Finally, we tested the hypothesis that RtxA13 contributes to human death caused by this zoonotic serovar by triggering an early cytokine storm in blood. To this end, we used a Bt2-SerE strain (R99) together with its rtxA13 deficient mutant, and a Bt1 strain (YJ016) producing RtxA11 (the most studied MARTXVv) together with its rtxA11 deficient mutant, as controls. Our results showed that RtxA13 was essential for virulence, as R99ΔΔrtxA13 was completely avirulent in our murine model of infection, and that R99, but not strain YJ016, induced an early, strong and dysregulated immune response involving the up-regulation of a high number of genes. This dysregulated immune response was directly linked to RtxA13. Based on these results and those obtained ex vivo (human blood), we propose a model of infection for the zoonotic serovar of V. vulnificus, in which RtxA13 would act as a sepsis-inducing toxin.


Subject(s)
Bacterial Toxins/metabolism , Cytokines/metabolism , Host-Pathogen Interactions , Sepsis/pathology , Vibrio vulnificus/immunology , Vibrio vulnificus/pathogenicity , Virulence Factors/metabolism , Animals , Cell Death/drug effects , Cells, Cultured , Disease Models, Animal , Endothelial Cells/drug effects , Endothelial Cells/physiology , Female , Humans , Mice, Inbred BALB C , Monocytes/drug effects , Monocytes/physiology , Sepsis/microbiology , Serogroup , Virulence
4.
Nature ; 532(7597): 64-8, 2016 Apr 07.
Article in English | MEDLINE | ID: mdl-27027296

ABSTRACT

Cytolytic proteins and peptide toxins are classical virulence factors of several bacterial pathogens which disrupt epithelial barrier function, damage cells and activate or modulate host immune responses. Such toxins have not been identified previously in human pathogenic fungi. Here we identify the first, to our knowledge, fungal cytolytic peptide toxin in the opportunistic pathogen Candida albicans. This secreted toxin directly damages epithelial membranes, triggers a danger response signalling pathway and activates epithelial immunity. Membrane permeabilization is enhanced by a positive charge at the carboxy terminus of the peptide, which triggers an inward current concomitant with calcium influx. C. albicans strains lacking this toxin do not activate or damage epithelial cells and are avirulent in animal models of mucosal infection. We propose the name 'Candidalysin' for this cytolytic peptide toxin; a newly identified, critical molecular determinant of epithelial damage and host recognition of the clinically important fungus, C. albicans.


Subject(s)
Candida albicans/metabolism , Candida albicans/pathogenicity , Cytotoxins/metabolism , Fungal Proteins/toxicity , Mycotoxins/toxicity , Virulence Factors/metabolism , Calcium/metabolism , Candida albicans/immunology , Candidiasis/metabolism , Candidiasis/microbiology , Candidiasis/pathology , Cell Membrane Permeability/drug effects , Cytotoxins/genetics , Cytotoxins/toxicity , Epithelial Cells/drug effects , Epithelial Cells/immunology , Epithelial Cells/pathology , Fungal Proteins/genetics , Fungal Proteins/metabolism , Host-Pathogen Interactions/immunology , Humans , Mucous Membrane/microbiology , Mucous Membrane/pathology , Mycotoxins/genetics , Mycotoxins/metabolism , Signal Transduction/drug effects , Virulence/drug effects , Virulence Factors/genetics , Virulence Factors/toxicity
5.
Front Biosci (Landmark Ed) ; 21(2): 278-302, 2016 01 01.
Article in English | MEDLINE | ID: mdl-26709773

ABSTRACT

Toll-like receptors (TLRs) constitute a family of pattern-recognition receptors (PRRs) that recognize molecular signatures of microbial pathogens and function as sensors for infection. Recognition of Candida albicans by TLRs on mature immune cells, such as phagocytic cells, activates intracellular signalling pathways that trigger production of proinflammatory cytokines which are critical for innate host defence and orchestrate the adaptive response. TLR2, and TLR4 in a minor extent, recognize cell wall-associated ligands; endosomal TLR9 and TLR7 recognize DNA and RNA respectively. Interaction of C. albicans with TLRs is a complex process, as TLRs may collaborate with other PRRs and expression of surface-associated fungal ligands depends on the strain and the morphotype (yeasts or hyphae), thus defining the final induced adaptive response (Th1/Th2/Th17). TLRs are also expressed on hematopoietic stem and progenitor cells (HSPCs) where they may play a role in modulating hematopoiesis; engagement of TLR2 induces, upon recognition of C. albicans, the differentiation of HSPCs towards specific subsets of mature myeloid cells. This has opened a new perspective for anti-Candida immunointervention.


Subject(s)
Candida albicans/isolation & purification , Candidiasis/physiopathology , Toll-Like Receptors/physiology , Animals , Candidiasis/immunology , Candidiasis/microbiology , Disease Susceptibility , Humans , Immunity, Innate , Mice
6.
Future Microbiol ; 10(4): 471-87, 2015.
Article in English | MEDLINE | ID: mdl-25865188

ABSTRACT

AIM: To demonstrate that Vibrio vulnificus, a sepsis-related aquatic pathogen, can provoke a strong pro-inflammatory reaction in blood-associated target cells. MATERIALS & METHODS: We selected two strains of the two main phylogenetic lineages, two human cell lines, monocytes and vascular endothelial cells and designed an in vitro infection model simulating early septicemia. RESULTS: Both strains caused a strong cell-specific pro-inflammatory response and produced a high degree of cell damage that ended with death by lysis (endothelial cells) or apoptosis/lysis (monocytes). The interaction with endothelial cells was stronger than expected and significantly different for both lineages. CONCLUSION: The early interaction with endothelial cells could have a direct role in sepsis and could explain, at least partially, the differences in pathogenicity between both lineages.


Subject(s)
Endothelial Cells/immunology , Endothelial Cells/microbiology , Host-Pathogen Interactions , Inflammation/physiopathology , Monocytes/immunology , Monocytes/microbiology , Vibrio vulnificus/physiology , Cells, Cultured , Gene Expression Profiling , Humans , Stress, Physiological
7.
PLoS One ; 9(5): e98077, 2014.
Article in English | MEDLINE | ID: mdl-24857971

ABSTRACT

The majority of HIV-1 infections worldwide are acquired via mucosal surfaces. However, unlike the vaginal mucosa, the issue of whether the oral mucosa can act as a portal of entry for HIV-1 infection remains controversial. To address potential differences with regard to the fate of HIV-1 after exposure to oral and vaginal epithelium, we utilized two epithelial cell lines representative of buccal (TR146) and pharyngeal (FaDu) sites of the oral cavity and compared them with a cell line derived from vaginal epithelium (A431) in order to determine (i) HIV-1 receptor gene and protein expression, (ii) whether HIV-1 genome integration into epithelial cells occurs, (iii) whether productive viral infection ensues, and (iv) whether infectious virus can be transferred to permissive cells. Using flow cytometry to measure captured virus by HIV-1 gp120 protein detection and western blot to detect HIV-1 p24 gag protein, we demonstrate that buccal, pharyngeal and vaginal epithelial cells capture CXCR4- and CCR5-utilising virus, probably via non-canonical receptors. Both oral and vaginal epithelial cells are able to transfer infectious virus to permissive cells either directly through cell-cell attachment or via transcytosis of HIV-1 across epithelial cells. However, HIV-1 integration, as measured by real-time PCR and presence of early gene mRNA transcripts and de novo protein production were not detected in either epithelial cell type. Importantly, both oral and vaginal epithelial cells were able to support integration and productive infection if HIV-1 entered via the endocytic pathway driven by VSV-G. Our data demonstrate that under normal conditions productive HIV-1 infection of epithelial cells leading to progeny virion production is unlikely, but that epithelial cells can act as mediators of systemic viral dissemination through attachment and transfer of HIV-1 to permissive cells.


Subject(s)
Epithelial Cells/virology , HIV-1/physiology , Mouth Mucosa/cytology , Vagina/cytology , Cell Line , DNA, Viral/genetics , DNA, Viral/metabolism , Epithelial Cells/metabolism , Female , Gene Expression Regulation , Genome, Viral/genetics , HIV-1/genetics , HIV-1/metabolism , Humans , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Cell Surface/metabolism , Transcription, Genetic , Viral Proteins/biosynthesis , Viral Proteins/genetics , Virus Integration
8.
J Infect Dis ; 209(11): 1816-26, 2014 Jun 01.
Article in English | MEDLINE | ID: mdl-24357630

ABSTRACT

BACKGROUND: The ability of epithelial cells (ECs) to discriminate between commensal and pathogenic microbes is essential for healthy living. Key to these interactions are mucosal epithelial responses to pathogen-induced damage. METHODS: Using reconstituted oral epithelium, we assessed epithelial gene transcriptional responses to Candida albicans infection by microarray. Signal pathway activation was monitored by Western blotting and transcription factor enzyme-linked immunosorbent assay, and the role of these pathways in C. albicans-induced damage protection was determined using chemical inhibitors. RESULTS: Transcript profiling demonstrated early upregulation of epithelial genes involved in immune responses. Many of these genes constituted components of signaling pathways, but only NF-κB, MAPK, and PI3K/Akt pathways were functionally activated. We demonstrate that PI3K/Akt signaling is independent of NF-κB and MAPK signaling and plays a key role in epithelial immune activation and damage protection via mammalian target of rapamycin (mTOR) activation. CONCLUSIONS: PI3K/Akt/mTOR signaling may play a critical role in protecting epithelial cells from damage during mucosal fungal infections independent of NF-κB or MAPK signaling.


Subject(s)
Candida albicans/physiology , Epithelial Cells/microbiology , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-akt/metabolism , TOR Serine-Threonine Kinases/metabolism , Cell Line, Tumor , Epithelial Cells/metabolism , Gene Expression Regulation/immunology , Humans , Hyphae , Phosphatidylinositol 3-Kinases/genetics , Protein Array Analysis , Proto-Oncogene Proteins c-akt/genetics , Signal Transduction/immunology , TOR Serine-Threonine Kinases/genetics , Transcriptome
9.
Exp Eye Res ; 110: 125-35, 2013 May.
Article in English | MEDLINE | ID: mdl-23375594

ABSTRACT

Unlike fish and amphibians, mammals do not regenerate retinal neurons throughout life. However, neurogenic potential may be conserved in adult mammal retina and it is necessary to identify the factors that regulate retinal progenitor cells (RPC) proliferative capacity to scope their therapeutic potential. Müller cells can be progenitors for retinal neuronal cells and can play an essential role in the restoration of visual function after retinal injury. Some members of the Toll-like receptor (TLR) family, TLR2, TLR3 and TLR4, are related to progenitor cells proliferation. Müller cells are important in retinal regeneration and stable cell lines are useful for the study of retinal stem cell biology. Our purpose was to obtain a Müller-derived cell line with progenitor characteristics and potential interest in regeneration processes. We obtained and characterized a murine Müller-derived cell line (MU-PH1), which proliferates indefinitely in vitro. Our results show that (i) MU-PH1 cells expresses the Müller cell markers Vimentin, S-100, glutamine synthetase and the progenitor and stem cell markers Nestin, Abcg2, Ascl1, α-tubulin and ß-III-tubulin, whereas lacks the expression of CRALBP, GFAP, Chx10, Pax6 and Notch1 markers; (ii) MU-PH1 cell line stably express the photoreceptor markers recoverin, transducin, rhodopsin, blue and red/green opsins and also melanopsin; (iii) the presence of opsins was confirmed by the recording of intracellular free calcium levels during light stimulation; (iv) MU-PH1 cell line also expresses the melatonin MT1 and MT2 receptors; (v) MU-PH1 cells express TLR1, 2, 4 and 6 mRNA; (vi) MU-PH1 express TLR2 at cell surface level; (vii) Candida albicans increases TLR2 and TLR6 mRNA expression; (viii) C. albicans or TLR selective agonists (Pam(3)CysSK(4), LPS) did not elicit morphological changes nor TNF-α secretion; (ix) C. albicans and Pam(3)CysSK(4) augmented MU-PH1 neurospheres formation in a statistically significant manner. Our results indicate that MU-PH1 cell line could be of great interest both as a photoreceptor model and in retinal regeneration approaches and that TLR2 may also play a role in retinal cell proliferation.


Subject(s)
Neuroglia/cytology , Photoreceptor Cells/cytology , Retina/cytology , Stem Cells/cytology , Aniline Compounds/metabolism , Animals , Biomarkers/metabolism , Blotting, Western , Calcium/metabolism , Cell Line , Cell Proliferation , Eye Proteins/metabolism , Female , Flow Cytometry , Fluorescent Dyes/metabolism , Mice , Mice, Inbred C57BL , Neuroglia/metabolism , Photoreceptor Cells/metabolism , Reverse Transcriptase Polymerase Chain Reaction , Stem Cells/metabolism , Tumor Necrosis Factor-alpha/metabolism , Xanthenes/metabolism
10.
PLoS One ; 7(3): e33362, 2012.
Article in English | MEDLINE | ID: mdl-22428031

ABSTRACT

The fungus C. albicans uses adhesins to interact with human epithelial surfaces in the processes of colonization and pathogenesis. The C. albicans ALS (agglutinin-like sequence) gene family encodes eight large cell-surface glycoproteins (Als1-Als7 and Als9) that have adhesive function. This study utilized C. albicans Δals mutant strains to investigate the role of the Als family in oral epithelial cell adhesion and damage, cytokine induction and activation of a MAPK-based (MKP1/c-Fos) signaling pathway that discriminates between yeast and hyphae. Of the eight Δals mutants tested, only the Δals3 strain showed significant reductions in oral epithelial cell adhesion and damage, and cytokine production. High fungal:epithelial cell multiplicities of infection were able to rescue the cell damage and cytokine production phenotypes, demonstrating the importance of fungal burden in mucosal infections. Despite its adhesion, damage and cytokine induction phenotypes, the Δals3 strain induced MKP1 phosphorylation and c-Fos production to a similar extent as control cells. Our data demonstrate that Als3 is involved directly in epithelial adhesion but indirectly in cell damage and cytokine induction, and is not the factor targeted by oral epithelial cells to discriminate between the yeast and hyphal form of C. albicans.


Subject(s)
Cell Adhesion Molecules/metabolism , Epithelial Cells/metabolism , Fungal Proteins/metabolism , Mouth Mucosa/microbiology , Signal Transduction/genetics , Blotting, Western , Cytokines/metabolism , Dual Specificity Phosphatase 1/metabolism , Fungal Proteins/genetics , Humans , Mouth Mucosa/cytology , Mouth Mucosa/pathology , Phosphorylation , Proto-Oncogene Proteins c-fos/metabolism
11.
Med Microbiol Immunol ; 201(1): 93-101, 2012 Feb.
Article in English | MEDLINE | ID: mdl-21706283

ABSTRACT

Oral epithelial cells detect the human pathogenic fungus Candida albicans via NF-κB and a bi-phasic mitogen-activated protein kinase (MAPK) signaling response. However, discrimination between C. albicans yeast and hyphal forms is mediated only by the MAPK pathway, which constitutes activation of the MAPK phosphatase MKP1 and the c-Fos transcription factor and is targeted against the hyphal form. Given that C. albicans is not the only Candida species capable of filamentation or causing mucosal infections, we sought to determine whether this MAPK/MKP1/c-Fos mediated response mechanism was activated by other pathogenic Candida species, including C. dubliniensis, C. tropicalis, C. parapsilosis, C. glabrata and C. krusei. Although all Candida species activated the NF-κB signaling pathway, only C. albicans and C. dubliniensis were capable of inducing MKP1 and c-Fos activation, which directly correlated with hypha formation. However, only C. albicans strongly induced cytokine production (G-CSF, GM-CSF, IL-6 and IL-1α) and cell damage. Candida dubliniensis, C. tropicalis and C. parapsilosis were also capable of inducing IL-1α and this correlated with mild cell damage and was dependent upon fungal burdens. Our data demonstrate that activation of the MAPK/MKP1/c-Fos pathway in oral epithelial cells is specific to C. dubliniensis and C. albicans hyphae.


Subject(s)
Candida albicans/immunology , Candida/immunology , Epithelial Cells/metabolism , Hyphae/immunology , Mitogen-Activated Protein Kinases/metabolism , Mouth/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Candida/classification , Candida/growth & development , Candida/pathogenicity , Candida albicans/growth & development , Candida albicans/pathogenicity , Cell Line, Tumor , Cells, Cultured , Cytokines/metabolism , Dual Specificity Phosphatase 1/genetics , Dual Specificity Phosphatase 1/metabolism , Epithelial Cells/immunology , Epithelial Cells/microbiology , Epithelial Cells/pathology , Humans , Mitogen-Activated Protein Kinases/genetics , Mouth/cytology , Mouth/immunology , Mouth/pathology
12.
PLoS One ; 6(11): e26580, 2011.
Article in English | MEDLINE | ID: mdl-22087232

ABSTRACT

We previously reported that a bi-phasic innate immune MAPK response, constituting activation of the mitogen-activated protein kinase (MAPK) phosphatase MKP1 and c-Fos transcription factor, discriminates between the yeast and hyphal forms of Candida albicans in oral epithelial cells (ECs). Since the vast majority of mucosal Candida infections are vaginal, we sought to determine whether a similar bi-phasic MAPK-based immune response was activated by C. albicans in vaginal ECs. Here, we demonstrate that vaginal ECs orchestrate an innate response to C. albicans via NF-κB and MAPK signaling pathways. However, unlike in oral ECs, the first MAPK response, defined by c-Jun transcription factor activation, is delayed until 2 h in vaginal ECs but is still independent of hypha formation. The 'second' or 'late' MAPK response, constituting MKP1 and c-Fos transcription factor activation, is identical to oral ECs and is dependent upon both hypha formation and fungal burdens. NF-κB activation is immediate but independent of morphology. Furthermore, the proinflammatory response in vaginal ECs is different to oral ECs, with an absence of G-CSF and CCL20 and low level IL-6 production. Therefore, differences exist in how C. albicans activates signaling mechanisms in oral and vaginal ECs; however, the activation of MAPK-based pathways that discriminate between yeast and hyphal forms is retained between these mucosal sites. We conclude that this MAPK-based signaling pathway is a common mechanism enabling different human epithelial tissues to orchestrate innate immune responses specifically against C. albicans hyphae.


Subject(s)
Candida albicans/immunology , Epithelial Cells , Hyphae/immunology , MAP Kinase Signaling System/immunology , Vagina/microbiology , Chemokine CCL20 , Epithelial Cells/metabolism , Epithelial Cells/microbiology , Female , Granulocyte Colony-Stimulating Factor , Humans , Immunity, Innate , Interleukin-6 , Mouth Mucosa/immunology , Mouth Mucosa/microbiology , NF-kappa B/immunology , Vagina/immunology , Vagina/pathology
13.
Infect Immun ; 79(12): 4902-11, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21930756

ABSTRACT

Oral epithelial cells discriminate between the yeast and hyphal forms of Candida albicans via the mitogen-activated protein kinase (MAPK) signaling pathway. This occurs through phosphorylation of the MAPK phosphatase MKP1 and activation of the c-Fos transcription factor by the hyphal form. Given that fungal cell wall polysaccharides are critical in host recognition and immune activation in myeloid cells, we sought to determine whether ß-glucan and N- or O-glycosylation was important in activating the MAPK/MKP1/c-Fos hypha-mediated response mechanism and proinflammatory cytokines in oral epithelial cells. Using a series of ß-glucan and N- and O-mannan mutants, we found that N-mannosylation (via Δoch1 and Δpmr1 mutants) and O-mannosylation (via Δpmt1 and Δmnt1 Δmnt2 mutants), but not phosphomannan (via a Δmnn4 mutant) or ß-1,2 mannosylation (via Δbmt1 to Δbmt6 mutants), were required for MKP1/c-Fos activation, proinflammatory cytokine production, and cell damage induction. However, the N- and O-mannan mutants showed reduced adhesion or lack of initial hypha formation at 2 h, resulting in little MKP1/c-Fos activation, or restricted hypha formation/pseudohyphal formation at 24 h, resulting in minimal proinflammatory cytokine production and cell damage. Further, the α-1,6-mannose backbone of the N-linked outer chain (corresponding to a Δmnn9 mutant) may be required for epithelial adhesion, while the α-1,2-mannose component of phospholipomannan (corresponding to a Δmit1 mutant) may contribute to epithelial cell damage. ß-Glucan appeared to play no role in adhesion, epithelial activation, or cell damage. In summary, N- and O-mannosylation defects affect the ability of C. albicans to induce proinflammatory cytokines and damage in oral epithelial cells, but this may be due to indirect effects on fungal pathogenicity rather than mannose residues being direct activators of the MAPK/MKP1/c-Fos hypha-mediated immune response.


Subject(s)
Candida albicans/metabolism , Cell Wall/metabolism , Epithelial Cells/metabolism , Candida albicans/ultrastructure , Cell Line, Tumor , Cytokines/metabolism , Gene Expression Regulation/physiology , Genes, fos/physiology , Glycosylation , Humans , Inflammation/metabolism , Mannans/genetics , Mannans/metabolism , Mannose/metabolism , Mitogen-Activated Protein Kinase Kinases/genetics , Mitogen-Activated Protein Kinase Kinases/metabolism , Mitogen-Activated Protein Kinase Phosphatases/genetics , Mitogen-Activated Protein Kinase Phosphatases/metabolism
14.
FEMS Immunol Med Microbiol ; 63(1): 148-50, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21668824

ABSTRACT

We have investigated the expression of TLR2 and Dectin-1 in retinal microglia and their involvement in Candida albicans phagocytosis using a cytometric approach. The expression of both receptors has been demonstrated in CD11b(+) retinal cells. Phagocytosis of pHrodo-labelled C. albicans yeasts by microglial CD11b(+) cells of C57BL/6 mice was inhibited both by the Dectin-1 antagonist laminarin and anti-Dectin-1 antibodies, whereas phagocytosis of yeasts by retinal microglia of TLR2 KO mice was unaffected. These data indicate that phagocytosis of C. albicans yeasts by retinal microglia is mediated by Dectin-1, whereas TLR2 does not play a significant role in this process.


Subject(s)
Candida albicans/immunology , Membrane Proteins/immunology , Microglia/immunology , Nerve Tissue Proteins/immunology , Phagocytosis , Retina/immunology , Animals , CD11 Antigens/analysis , Gene Expression Profiling , Lectins, C-Type , Membrane Proteins/biosynthesis , Mice , Mice, Inbred C57BL , Mice, Knockout , Microglia/chemistry , Microglia/microbiology , Nerve Tissue Proteins/biosynthesis , Retina/microbiology , Toll-Like Receptor 2/biosynthesis , Toll-Like Receptor 2/immunology
15.
Cell Host Microbe ; 8(3): 225-35, 2010 Sep 16.
Article in English | MEDLINE | ID: mdl-20833374

ABSTRACT

Discriminating between commensal and pathogenic states of opportunistic pathogens is critical for host mucosal defense and homeostasis. The opportunistic human fungal pathogen Candida albicans is also a constituent of the normal oral flora and grows either as yeasts or hyphae. We demonstrate that oral epithelial cells orchestrate an innate response to C. albicans via NF-κB and a biphasic MAPK response. Activation of NF-κB and the first MAPK phase, constituting c-Jun activation, is independent of morphology and due to fungal cell wall recognition. Activation of the second MAPK phase, constituting MKP1 and c-Fos activation, is dependent upon hypha formation and fungal burdens and correlates with proinflammatory responses. Such biphasic response may allow epithelial tissues to remain quiescent under low fungal burdens while responding specifically and strongly to damage-inducing hyphae when burdens increase. MAPK/MKP1/c-Fos activation may represent a "danger response" pathway that is critical for identifying and responding to the pathogenic switch of commensal microbes.


Subject(s)
Candida albicans/immunology , Candida albicans/pathogenicity , Epithelial Cells/immunology , Epithelial Cells/microbiology , Mitogen-Activated Protein Kinases/metabolism , Mouth Mucosa/immunology , Mouth Mucosa/microbiology , Candida albicans/cytology , Candida albicans/growth & development , Candidiasis, Oral/immunology , Cell Line, Tumor , Cell Wall/immunology , Cytokines/metabolism , Dual Specificity Phosphatase 1/metabolism , Epithelial Cells/metabolism , Fungal Proteins/metabolism , Host-Pathogen Interactions , Humans , Hyphae/immunology , Mitogen-Activated Protein Kinase 1/metabolism , Mouth Mucosa/metabolism , NF-kappa B/metabolism , Proto-Oncogene Proteins c-fos/metabolism , Signal Transduction , Virulence , Yeasts/metabolism
16.
Cell Microbiol ; 12(1): 114-28, 2010 Jan.
Article in English | MEDLINE | ID: mdl-19747212

ABSTRACT

We have previously demonstrated that inactivated yeasts and hyphae of Candida albicans induce in vitro the proliferation of murine haematopoietic stem and progenitor cells (HSPCs, sorted as LKS cells: Lin(-) c-Kit(+) Sca-1(+)) as well as their differentiation to lineage-positive cells, through a MyD88-dependent pathway. In this work, we have found that this process is mainly mediated by TLR2, and that expanding cells express myeloid and not lymphoid markers. Incubation of long-term repopulating HSCs (Lin(-) CD105(+) and Sca-1(+)) with C. albicans yeasts resulted in their proliferation and up regulation of the common myeloid progenitors (CMPs) markers, CD34 and FcgammaRII/III, by a TLR2/MyD88-dependent signalling pathway. In addition, this TLR2/MyD88 signalling promotes the differentiation of CMPs and granulocyte and macrophage progenitors (GMPs) into cells with the morphology of macrophages and neutrophils, characterized by an increase in the expression of CD11b, F4/80 and Ly6G, independently of the presence of growth and differentiation factors. These differentiated cells were able to phagocytose C. albicans yeasts and to produce proinflammatory cytokines. In conclusion, C. albicans may be sensed by TLRs on haematopoietic stem and progenitor cells to promote the host capability for rapidly replenishing myeloid cells that constitute the first line of defence against C. albicans.


Subject(s)
Bone Marrow Cells/cytology , Candida albicans/physiology , Cell Differentiation , Myeloid Differentiation Factor 88/metabolism , Phagocytes/cytology , Stem Cells/cytology , Toll-Like Receptor 2/metabolism , Animals , Antigens, Differentiation/metabolism , Antigens, Ly/metabolism , CD11b Antigen/metabolism , Cells, Cultured , Flow Cytometry , Mice , Mice, Mutant Strains , Phagocytes/metabolism , Signal Transduction , Toll-Like Receptor 2/genetics
17.
Microbes Infect ; 11(4): 531-5, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19217944

ABSTRACT

As TLRs are expressed by hematopoietic stem and progenitor cells, these receptors may play a role in hematopoiesis in response to pathogens during infection. We showed here that inactivated yeasts and hyphae of Candida albicans induce in vitro the proliferation of purified murine hematopoietic stem and progenitor cells (Lin(-)c-Kit(+) Sca-1(+)) as well as their differentiation to lineage positive cells, through a MyD88-dependent pathway. These results indicate that TLR-mediated recognition of C. albicans by hematopoietic stem and progenitor cells may augment the host capability for rapidly replenishing the innate immune system during candidiasis.


Subject(s)
Candida albicans/physiology , Cell Differentiation , Cell Proliferation , Hematopoietic Stem Cells/physiology , Myeloid Differentiation Factor 88/metabolism , Stem Cells/physiology , Animals , Mice , Mice, Inbred C57BL
18.
FEMS Immunol Med Microbiol ; 53(2): 214-21, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18445021

ABSTRACT

Previous work by our group showed that aged C57BL/6 mice develop an altered innate and adaptive immune response to Candida albicans and are more susceptible to systemic primary candidiasis. In this work, we used young (2-3 months old) and aged (18-20 months old) C57BL/6 mice to study in vitro the influence of aging on (1) the fungicidal activity of neutrophils and macrophages, (2) the production of cytokines by resident peritoneal macrophages in response to C. albicans, and (3) cell surface Toll-like receptor (TLR) 2 expression on resident peritoneal macrophages. Our results indicate that murine phagocytes have a fungicidal activity well preserved with aging. In vitro production of proinflammatory cytokines (IL-6, IL-1beta, and tumor necrosis factor-alpha and chemokines (MIP-2) by purified (CD11b(+)) peritoneal macrophages in response to yeasts and hyphae of C. albicans was significantly lower in aged mice as compared with young mice. However, the production of IL-10 by macrophages, in response to C. albicans, was similar in both young and aged animals. Moreover, baseline TLR2 surface expression level was lower on aged macrophages than on control macrophages. Taken together, these data indicate that the increased susceptibility to C. albicans disseminated infections in aged mice is correlated with defects in TLR2 expression and in cytokine production, but not with an impaired fungicidal activity.


Subject(s)
Aging , Candida albicans/immunology , Macrophages, Peritoneal/immunology , Neutrophils/immunology , Animals , Cells, Cultured , Cytokines/biosynthesis , Female , Macrophages, Peritoneal/chemistry , Mice , Mice, Inbred C57BL , Microbial Viability/immunology , Phagocytosis , Toll-Like Receptors/analysis
19.
Microbes Infect ; 10(4): 382-9, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18403244

ABSTRACT

The Candida albicans gpi7/gpi7 null mutant strain (Deltagpi7), which is affected in glycosylphosphatidylinositol (GPI) anchor biosynthesis, showed a reduced virulence following systemic infection of C57BL/6 mice. In vitro production of TNF-alpha, IL-6 and IL-1beta by macrophages in response to Deltagpi7 cells was significantly increased as compared to control (wild type GPI7/GPI7 and revertant gpi7/GPI7) cells; this probably contributes to the enhanced recruitment of neutrophils to the peritoneal cavity in response to Deltagpi7 cells. Survival of knockout mice for Toll-like receptor (TLR) 2 and TLR4 following intravenous injection of Deltagpi7 cells showed no significant differences as compared to C57BL/6 mice. In vitro production of TNF-alpha by macrophages and neutrophil recruitment were significantly inhibited in TLR2-/- mice in response to control yeast strains. Interestingly both TNF-alpha production and neutrophil recruitment in response to Deltagpi7 were significantly increased in all three types of mice, with no differences among them, and laminarin failed to inhibit this increased production of TNF-alpha. These results indicate that the enhanced proinflammatory response to Deltagpi7 does not involve recognition through TLR2, TLR4 nor dectin-1. Therefore, complete GPI anchors confer surface properties that are involved in modulation of cytokine production by macrophages in response to C. albicans.


Subject(s)
Candida albicans/genetics , Candida albicans/immunology , Fungal Proteins/genetics , Fungal Proteins/immunology , Glycosylphosphatidylinositols/immunology , Inflammation/immunology , Inflammation/microbiology , Animals , Cells, Cultured , Gene Deletion , Glycosylphosphatidylinositols/genetics , Interleukin-1beta/biosynthesis , Interleukin-6/biosynthesis , Macrophages, Peritoneal/immunology , Macrophages, Peritoneal/microbiology , Mice , Mice, Inbred C57BL , Mice, Knockout , Neutrophils/immunology , Peritoneal Cavity/pathology , Survival Analysis , Toll-Like Receptor 2/deficiency , Toll-Like Receptor 4/deficiency , Tumor Necrosis Factor-alpha/biosynthesis , Virulence , Virulence Factors/genetics , Virulence Factors/immunology
20.
FEMS Immunol Med Microbiol ; 51(2): 327-35, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17714490

ABSTRACT

Invasive infections with opportunistic fungi, such as Candida albicans, have become an increasing problem in aged adults in recent years. This work investigates the influence of human ageing on C. albicans recognition by toll-like receptors (TLRs), essential components of the innate immune system, using a cohort of 96 young (15-42 years) and aged (>70 years) human volunteers. No significant differences between aged and young donors were observed on (1) cell surface TLR2, TLR6 and TLR4 expression on lymphocytes, monocytes and granulocytes, (2) production of cytokines [IL-8, IL-1beta, IL-6, IL-10, tumour necrosis factor (TNF)-alpha and IL-12p70] and prostaglandin E(2) (PGE(2)) by whole human blood in response to C. albicans and (3) fungicidal activity of whole blood. A statistically significant higher titre of natural anti-C. albicans antibodies was found in plasma of volunteers between 80 and 95 years old when compared with other age groups, probably as a consequence of the increased levels of serum Ig that has been described in elderly subjects. Therefore, the results indicate that the increased susceptibility to C. albicans infections in the elderly is not a consequence of defects in TLRs expression or signalling, nor of an impaired fungicidal activity of blood.


Subject(s)
Candida albicans/immunology , Adolescent , Adult , Age Factors , Aged , Aged, 80 and over , Antibodies, Fungal/blood , Blood/immunology , Cytokines/biosynthesis , Dinoprostone/biosynthesis , Female , Granulocytes/chemistry , Humans , Lymphocytes/chemistry , Male , Microbial Viability , Monocytes/chemistry , Toll-Like Receptor 2/analysis , Toll-Like Receptor 4/analysis , Toll-Like Receptor 6/analysis
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